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PRE-084

С Википедије, слободне енциклопедије
PRE-084
IUPAC ime
2-morpholin-4-ylethyl 1-phenylcyclohexane-1-carboxylate
Identifikatori
CAS broj138847-85-5 ДаY
ATC kodnone
PubChemCID 126402
Hemijski podaci
FormulaC19H27NO3
Molarna masa317.422 g/mol
  • c1ccccc1C2(CCCCC2)C(=O)OCCN3CCOCC3

PRE-084 je agonist sigma receptor, koji je selektivan za σ1 tip. On je pokazao nootropno i antidepresivno dejstvo u studijama na životinjama, da može da služi kao sredstvo protiv kašlja.[1][2][3][4][5] PRE-084 povišava GDNF izražavanje.[6]

  1. ^ Maurice T, Su TP, Parish DW, Nabeshima T, Privat A (1994). „PRE-084, a sigma selective PCP derivative, attenuates MK-801-induced impairment of learning in mice”. Pharmacology, Biochemistry, and Behavior. 49 (4): 859—69. PMID 7886099. S2CID 54306053. doi:10.1016/0091-3057(94)90235-6. 
  2. ^ Maurice T (2001). „Beneficial effect of the sigma(1) receptor agonist PRE-084 against the spatial learning deficits in aged rats”. European Journal of Pharmacology. 431 (2): 223—7. PMID 11728429. doi:10.1016/s0014-2999(01)01436-4. 
  3. ^ Brown C, Fezoui M, Selig WM, Schwartz CE, Ellis JL (2004). „Antitussive activity of sigma-1 receptor agonists in the guinea-pig”. British Journal of Pharmacology. 141 (2): 233—40. PMC 1574192Слободан приступ. PMID 14691051. doi:10.1038/sj.bjp.0705605. 
  4. ^ Skuza G, Rogóz Z (2009). „Antidepressant-like effect of PRE-084, a selective sigma1 receptor agonist, in Albino Swiss and C57BL/6J mice”. Pharmacological Reports : PR. 61 (6): 1179—83. PMID 20081254. S2CID 96025873. doi:10.1016/s1734-1140(09)70181-1. 
  5. ^ Hiranita T, Soto PL, Tanda G, Katz JL (2010). „Reinforcing effects of sigma-receptor agonists in rats trained to self-administer cocaine”. The Journal of Pharmacology and Experimental Therapeutics. 332 (2): 515—24. PMC 2812106Слободан приступ. PMID 19892920. doi:10.1124/jpet.109.159236. 
  6. ^ Penas, C.; Pascual-Font, A.; Mancuso, R.; Forés, J.; Casas, C.; Navarro, X. (2011). „Sigma receptor agonist 2-(4-morpholinethyl)1 phenylcyclohexanecarboxylate (Pre084) increases GDNF and BiP expression and promotes neuroprotection after root avulsion injury”. Journal of Neurotrauma. 28 (5): 831—840. PMID 21332255. doi:10.1089/neu.2010.1674. 


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